Optimization for Toric Contact Lenses
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCooperVision International Limited (CVIL)
About this trial
The aim of this study is to evaluate the agreement between subjective and objective toric lens prescriptions.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
They are at least 18 years of age.
They understand their rights as a research participant and are willing and able to sign a Statement of Informed Consent.
They have spherical refractive error at the corneal plane between +4.00 to -7.00DS
They have refractive astigmatism at the corneal plane of 0.75 to 2.25DC in one eye.
Disqualifiers
Is participating in any concurrent clinical or research trial.
They have an ocular disorder which would normally contra-indicate contact lens wear.
They have a systemic disorder which would normally contra-indicate contact lens wear.
They are pseudophakic or aphakic.
Trial design
Design model
Parallel
Treatments tested in this trial
Lens 1 ( stenfilcon A )
Device15 minutes of daily wear
Lens 2 ( comfilcon A )
Device15 minutes of daily wear
Treatment groups
45 Participants
are divided into 2 treatment groupsGroup A: Lens 1 ( stenfilcon A)Experimental treatment 1 intervention
Group B: Lens 2 ( comfilcon A)Experimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Subjective assessment of optimization of Toric lenses
Proportion of eyes in which the optimized toric lens cylinder axis determined by the subjective method agrees with that determined by the objective method within ±10 degrees (measured at a single time point).
Time frame
At the End of Baseline 15 minutes of daily wearSponsors and contacts
Click on the lead sponsor to view all of their trials.
CooperVision International Limited (CVIL)
Lead sponsor
Indiana University
Collaborator
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: